08-03 IPSEN - Buy-back programme - Art 5 of MAR - Week 31 - 2026 GL
08-03 Jefferies Downgrades Ipsen to Underperform, Boosts PT MT
07-31 Ipsen S.A., H1 2026 Earnings Call, Jul 30, 2026
07-30 Ipsen S.A. publishes its 2026 Half-Year Report (half-year ended 30 June 2026) GL
07-30 Ipsen: Another quarterly beat; 2026 guidance upgraded Alphavalue
07-30 Ipsen S.A. Reports Earnings Results for the Half Year Ended June 30, 2026 CI
07-30 Ipsen raises its full-year targets Zonebourse
07-30 Ipsen Raises FY26 Sales Growth Outlook MT
07-30 Ipsen delivers excellent H1 2026 results and upgrades its full-year guidance GL
07-29 Ipsen nominates Catherine Bradley to its Board of Directors as independent Director GL
07-29 Ipsen Announces Appointment of Catherine Bradley, CBE, as an Independent Director, Chair of the Audit Committee and Member of the Compensation Committee, Effective July 29, 2026 CI
07-27 IPSEN - Buy-back programme - Art 5 of MAR - Week 30 - 2026 GL
07-24 Ipsen Provides Update On Phase III BOLD Trial In Biliary Atresia CI
07-24 Ipsen Says Phase 3 Trial of Bylvay in Biliary Atresia Misses Primary Endpoint MT
07-24 Ipsen provides update on Phase III BOLD trial in biliary atresia GL
07-22 Ipsen Closes Purchase of Potravitug Developer Memo Therapeutics MT
07-22 Ipsen completes acquisition of Memo Therapeutics AG, adding first-in-class asset to Ipsen's Rare Disease pipeline GL
07-21 Ipsen S.A. acquired Memo Therapeutics AG. CI
07-21 IPSEN - Buy-back programme - Art 5 of MAR - Week 29 - 2026 GL
07-15 IPSEN - Buy-back programme - Art 5 of MAR - Week 28 - 2026 GL
07-13 Positive news for Ipsen's Iqirvo Zonebourse
07-13 Ipsen : IQIRVO® demonstrates statistically significant improvement in ALP normalization in patients with PBC in Phase IIIb ELSPIRE study PU
07-10 Ipsen - Dysport is the first botulinum toxin to achieve positive topline Phase III results in both episodic and chronic migraine AQ
07-09 Ipsen Reports Positive Topline Phase III Results for Dysport in Both Episodic and Chronic Migraine CI
07-09 Ipsen's Migraine Treatment Meets Primary Endpoints in Late-stage Trial MT
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